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21ohd diagnosis disease endocrinology genetics pathophysiology peds rheumatology syndrome
21-Hydroxylase Deficiency (21-OHD): Pathogenesis and Clinical Findings Autosomal recessive mutation in CYP21A2 coding for the enzyme 21-OHase
Signs/Symptoms/Complications ... vomiting • Late (shock ... a scrotum #21HydroxylaseDeficiency ... endocrinology #peds #pediatrics
Behçet's Syndrome Systemic disease associated with inflammation of multiple organs, small-vessel vasculitis and large-vessel vasculopathy Epidemiology: • Young
meningitis), MCC CNS symptoms ... azathioprine #Behcet ... Syndrome #diagnosis #management ... #signs #symptoms ... #rheumatology #
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